A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350076



Internal ID21007629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45059682..45108135hg38UCSC Ensembl
chr2:45286821..45335274hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3848454
hg1948454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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